Veikko Salomaa
Nature Genetics · 2005–2023
A researcher in the Science corpus: 73 papers; trusts 0 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Who trusts Veikko Salomaa
- Chris Wallace (in Genetics)
Papers from Veikko Salomaa's perspective
Ordered by how strongly the researchers Veikko Salomaa trusts endorse each paper. Same corpus, a different order for every researcher.
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
- Next-generation genotype imputation service and methods (Nature Genetics)
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
- A gene-based association method for mapping traits using reference transcriptome data (Nature Genetics)
- FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
- An expanded view of complex traits: from polygenic to omnigenic (Cell)
- Estimating the Dimension of a Model
- Bayesian variable selection regression for genome-wide association studies and other large-scale problems
- Monte Carlo Sampling Methods Using Markov Chains and Their Applications
- Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood (Bioinform.)
Their papers
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) — 1,982 citations
- Systematic identification of trans-eQTLs as putative drivers of known disease associations (2013) — 1,732 citations
- FINEMAP: efficient variable selection using summary data from genome-wide association studies (2015) — 774 citations
- Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants (2009) — 1,094 citations
- The transcriptional landscape of age in human peripheral blood (2015) — 654 citations
- Identification of ten loci associated with height highlights new biological pathways in human growth (2008) — 644 citations
- A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) — 1,284 citations
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- Large-scale association analysis identifies new risk loci for coronary artery disease (2012) — 1,642 citations
- A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease (2015) — 2,034 citations
- Genome-wide meta-analyses identify multiple loci associated with smoking behavior (2010) — 1,140 citations
- Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA (2016) — 691 citations
- Association of Cardiometabolic Multimorbidity With Mortality. (2015) — 954 citations
- Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population (2014) — 412 citations
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) — 162 citations
- Greengenes2 unifies microbial data in a single reference tree (2023) — 563 citations
- FinnGen provides genetic insights from a well-phenotyped isolated population (2023) — 3,553 citations
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) — 2,226 citations
- SCORE2 risk prediction algorithms: new models to estimate 10-year risk of cardiovascular disease in Europe. (2021) — 1,383 citations
- The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations